# Senior Strategist - Regulatory Affairs (CMC) at ClinChoice

> India · Senior · Other · open. Source: https://alderhq.app/jobs/greenhouse%3Aclinchoice%3A4938438101 (read 2026-11-15).

## Facts (observed)

- Company: [ClinChoice](https://alderhq.app/companies/clinchoice)
- Location text: City, State/County - Country ; India
- Where it can be done from (inferred): India (evidence: "Location lists "india"")
- Posted: 2026-09-25 (51 days ago)
- First seen by alder: 2026-11-04 · last verified: 2026-11-13
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: https://job-boards.eu.greenhouse.io/clinchoice/jobs/4938438101

## Pay and sponsorship

- Posted pay: not posted
- Market band for similar posted roles (India, n 9): p25 ₹12.2L, median ₹16.6L, p75 ₹29.5L
- Licensed UK sponsor: registered as "CLINCHOICE LIMITED" (checked 2026-11-15, [register](https://www.gov.uk/government/publications/register-of-licensed-sponsors-workers))

## Description (the employer's text)

### Responsibilities

- Manage the preparation and submission of new product registrations, post approval submission, and follow-up closely on queries and through approval
- Responsible for reviewing and writing CMC modules 2 and 3
- Exposure to EU and CIS region in regulatory filings
- Herbal product development background
- Manage and coordinate product life cycle management
- Ensure regulatory compliance with local regulatory requirements
- Foster and maintain professional relationships with the health authorities
- Provide regulatory support including timely registration of new product and line extensions to support new product launches and tender applications when necessary
- Maintain regulatory work processes and tracking tools that improve performance levels and transparency
- Exposure in writing of Product Quality Review
- Promote regulatory intelligence in both local and regional initiatives
- Develop regulatory strategies, prepare regulatory applications, and support maintenance activities within relevant therapy areas
- Execution of regulatory strategies (local and regional) that are in line with the business plan
- Complete regulatory activities for a defined number of products to ensure all regulatory obligations and business objectives are met
- Ensure adherence to timelines and quality set parameters R
- eview of formulation, generation of ingredient list, and claims per set standards
- Compilation and review of labeling components per SOP
### Deliverables

- CMC modules 2 and 3
- Management of the preparation and submission of new product registrations, post approval submissions, and follow-up on queries through approval
- Review of CMC modules
- Execution of regulatory strategies (local and regional) that are in line with the business plan
- Compilation of PQR as per SOP – Summary report of variations submitted as per the specified period.
- Review of formulation, generation of ingredient list, and claims per set standards
- Compilation and review of labeling components per SOP
### Experience/Qualifications

- Bachelor’s/Master’s degree in Life Science/Pharma
- Six to eight years of relevant work experience
- RAPS certification is desirable

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/greenhouse%3Aclinchoice%3A4938438101 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.